TY  - GEN
AU  - Courtens,W
AU  - Tjalma,W
AU  - Messiaen,L
AU  - Vamos,E
AU  - Martin,J J
AU  - Van Bogaert,E
AU  - Keersmaekers,G
AU  - Meulyzer,P
AU  - Wauters,J
TI  - Prenatal diagnosis of a constitutional interstitial deletion of chromosome 5 (q15q31.1) presenting with features of congenital contractural arachnodactyly
SN  - 0148-7299
PY  - 1998///0709
KW  - Abnormalities, Multiple
KW  - diagnosis
KW  - Abortion, Induced
KW  - Adult
KW  - Chromosome Deletion
KW  - Chromosomes, Human, Pair 5
KW  - Clubfoot
KW  - diagnostic imaging
KW  - Connective Tissue Diseases
KW  - congenital
KW  - Contracture
KW  - DNA
KW  - blood
KW  - Female
KW  - Fetal Diseases
KW  - Fibrillin-2
KW  - Fibrillins
KW  - Humans
KW  - In Situ Hybridization, Fluorescence
KW  - Karyotyping
KW  - Male
KW  - Marfan Syndrome
KW  - Microfilament Proteins
KW  - genetics
KW  - Pregnancy
KW  - Prenatal Diagnosis
KW  - Ultrasonography, Prenatal
N1  - Publication Type: Case Reports; Journal Article
ER  -